- Total grants
- Total funders
- Total recipients
- Earliest award date
- 17 Oct 2005
- Latest award date
- 30 Sep 2018
- Total GBP grants
- Total GBP awarded
- Largest GBP award
- Smallest GBP award
- Total Non-GBP grants
HIV/AIDS amongst Britain's African communities is a major public health concern, yet to date, relatively little research has focused on this group. This study will increase our understanding of the factors which influence access to, and utilisation of, HIV treatment and prevention services among African communities in Britain. It will also help to inform the development of culturally appropriate HIV health promotion interventions aimed at increasing service uptake within these communities. Plan of investigation: The study population will be all African patients attending in- or outpatient services at selected London HIV treatment centres. To date 7 centres have agreed to participate. The project will consist of two inter-linked components implemented over 2 years: i) A qualitative study amongst a purposively selected sample of newly diagnosed HIV positive Africans employing in-depth interview techniques, and ii) A cross-sectional survey of newly diagnosed HIV positive Africans presenting to specialist HIV services in London. Key workers at each study site will recruit patients and distribute the questionnaires. Dr Burns will perform the interviews. 'Framework' will be used for organising and analysing the qualitative research. Quantitative data analysis will be using STATA 6.0. The questionnaire, topic guide and protocol will be submitted to all appropriate Research Ethics Committees for approval. All patients will be given written information regarding the study and written informed consent will be obtained prior to participation. An African Community Reference Group will be set up to oversee all stages of the study design. Background preparation for the study will be undertaken as part of the MSc dissertation. Study outputs: Peer reviewed publication on health care seeking behaviours among Africans and reasons for delayed presentation; contextual information on healthcare access and utilisation, stigma, onward HIV transmission risk and proportion of HIV infections acquired within the UK.
Malnutrition has a major impact on the health of children and is responsible for approximately 50% of all childhood deaths, mostly from infectious disease. The precise relationship between malnutrition, immune competence and infectious disease is poorly understood, yet these interrelated factors are the critical determinants of childhood morbidity and mortality. Though neglected in recent years, the association of malnutrition with defects in cell mediated immunity (CMI) is well established. Studies of CMI in malnutrition have focused on T cells, however, central to the successful generation of T cell responses is the ability of the host to present antigen to T cells. The professional antigen presenting cell in humans is the dendritic cell (DC), yet DCs have not been studied in any great detail in malnutrition, partly because the technology for their isolation and culture have only recently been established. Abnormalities of DCs have been described in early life and in association with infections such as HIV and malaria. T cell abnormalities described in severe malnutrition may be secondary to abnormalities of DCs. We propose to study DC function in a group of severely malnourished children on admission to a nutrition ward and then follow their DC function through recovery. The chosen study site in Zambia provides the ideal environment for such a study as the nutrition ward at Lusaka University Teaching Hospital admits 1,800 severely malnourished children a year and has an active research unit. During the study we will (1) characterise the patterns of DC phenotype and function in severe malnutrition, (2) describe the effects of severe malnutrition, HIV and measles on DC function, and (3) describe the impact on DC function of in vitro supplementation with micronutrients, thought to contribute to DC function. This study will provide insights into the mechanism of immune deficiency in malnutrition while also providing a rational basis for the development of novel focused micronutrient supplementation aimed at improving immune function in the severely malnourished child.
The FIL is a prime example of a UK based laboratory that is an established world leader. This application for a Strategic Award is motivated by the need to secure the future of the FIL. The FIL supports a large portfolio of Wellcome Trust (WT) supported programme and project grant research, fellowships and studentships. A Strategic Award will enable the laboratory to retain its highly-skilled core infrastructure support staff; ensure a context of excellence to enable Wellcome Trust funded principal investigators (PIs) to continue producing science that is world class and high impact; and enable the laboratory to provide specific added value. A key example of the latter is in the field of bio-mathematics and data-analysis where our goal is to provide a common platform (extended SPM) for integrating data across distinct imaging modalities including fMRI, magneto-encephalography (MEG) and electro-encephalography (EEG). Finally, a Strategic Award will enable the FIL to provide a theoretical-neuroscience framework that informs both basic and clinically-oriented research into common neurological and psychiatric diseases.
Conversation Piece. 26 Jul 2006
The Listening Room The Listening Room is a collaboration between artist Alexa Wright and Alf Linney, Professor of Medical Physics at University College London. Within the Centre for Auditory Research at UCL Alexa and Alf are researching an effective means of modelling human communication. With a view to creating an interactive audio installation - an intelligent room that can converse with its occupants - they will bring the latest technologies for sound placement and for speech recognition and synthesis into a clinical environment where they will interact with scientists who are working to understand the physical and neurological aspects of binaural hearing.
Neurotopographics. 26 Jul 2006
Neurotopographics The project brings together a scientist, an architect and an artist to make a film exploring how dynamic patterns of brain activity provide a code for the structure of space. The film will follow the journey of a visitor to an art gallery as seen through the visitor's eyes and from a bird's eye view on an architectural plan. During the journey the activity of brain cells known as 'place cells', 'grid cells' and 'head direction cells' will then be conveyed through a confrontation with sound and colour. The film will invite the audience to consider how their brains represent the world around them.
Volunteers in Biomedical Research: Social Science Perspectives The aim of this meeting is to bring together academics who are specifically interested in exploring what it means to be a volunteer from the volunteers' perspective. While many of the researchers in the field are London-based, there has been little opportunity for all to meet in a single forum. The workshop will develop ideas and collaborative links for future work, build capacity in the UK social science community, and explore how this area of research can engage with current debates in science policy and research governance. Although UK government policy now puts a strong emphasis on public participation in research governance, there remains little discussion on the participatory role of volunteer human subjects. There are questions too about how adequately current codes of medical ethics function in practice and how they can accommodate the idea of more actively participative volunteers. The proposed workshop and its outputs could contribute to moving forward these issues. Topics to be addressed will include: the researcher-subject relationship; volunteers' understandings of research design and the implications for informed consent; volunteer motivation to participate; historical perspectives on volunteers' self-understanding; the significance of discourse around the 'volunteer', 'participant' or 'subject'; the possibilities for volunteers to influence the design and development of research. The meeting fits specifically with the objective of the Wellcome Biomedical Ethics programme to "build and enhance national capacity in the field". Some of the invited participants are working specifically within the programme's focus, looking at volunteering in relation to genetics (especially genetic databases) and neuroscience (especially brain imaging); others are working on the role of volunteers in a diverse range of the biomedical sciences. This meeting is specifically concerned with qualitative studies of volunteers' own experiences and understandings, and to this extent we are not aware of any recent meetings on this emerging field of science.
'Epidemics in South Asian History: A review of medical, political and social responses' conference to be held in Burdwan, India on 7th, 8th and 9th November 2006. 08 Feb 2006
Epidemics in South Asian History: A review of medical, political and social responses A lot of the valuable research that this meeting will showcase is being carried out by staff in the smaller South Asian universities, whose contributions are often ignored in well-known publications; similarly, many UK-based associations for the study of the history of medicine remain unaware of the range and richness of this work, generally to their own disadvantage. This situation generally exists because scholars attached to the smaller South Asian universities have relatively weak links with the major international communities of historians of medicine, particularly those in the UK and Europe, where there has been a great interest in the subject over the past two decades. Apart from seeking to redress this situation, the proposed meeting also aims to highlight the significance of the study of the history of medicine at a university where a notable level of commitment towards the subject already exists. A joint meeting with the Wellcome Trust Centre would help advertise Burdwan University's efforts to propagate the post-graduate study of the history of medicine, science and technology, which would be useful both nationally and internationally. It is hoped that Burdwan University's efforts will receive greater publicity through a major international conference, which is likely to stoke greater government support for these educational ventures (activities in Burdwan University do not go unnoticed by the Government of West Bengal, which funds educational activities through the state). Burdwan University's intellectual resources could be useful to UK-based historians of medicine, as it offers the possibility of creating new collaborations and an effective base for Wellcome Trust-funded scholars seeking to carry out research in the region (research visas need to be sponsored by recognised universities and the university's department of history could be very helpful in this regard). Burdwan's history department is in keeping with the Wellcome Trust Centre agenda of seeking to expand interest in the history of medicine internationally; a goal in sync with the Wellcome Trust's history of medicine division's own goals.
A combinatorial approach using steroidgenic factor-1 (SF-1, NR5A1) to elucidate novel mechanisms in adrenal and reproductive biology. 05 Jun 2006
We aim to elucidate novel molecular mechanisms involved in human adrenal and reproductive development, and to relate these findings to patients with disorders of adrenal and reproductive function and to variations within normalpopulations. Using microarray and proteomic approaches, we now have the capacity to identify many of the components involved in these systems: the challenge is to focus on those factors relevant to human disease. We will address this using a combinatorial approach (Aims 1-3). In Aim 1, key differentially expressed genes/proteins will be identified in the adrenal, testis and ovary at critical stages of human development between 6-12 weeks gestation. In Aim 2, a subset of important novel genes will be identified by manipulation of the pivotal nuclear receptor sterodiogenic factor-1 (SF-1). InAim 3, genetic loci containing potentially important genes will be mapped using "literature mining" techniques and array analysis of patients with adrenal and reproductive disorders. Taken together, these studies will provideinsight into important biological mechanisms of development and function. Analysis of candidate factors in patients/families with adrenal and reproductive disorders will define novel endocrine syndromes and should identify key factors important in milder clinical phenotypes or physiological variability within a "normal" population (Aim 4).
Vesicle dynamics and synaptic computation. 01 Jun 2006
This proposal aims to build a quantitative understanding of synaptic function by providing direct links between molecular mechanisms and synaptic computation. We will focus mainly on the cerebellar mossy fibre-granule cell synapse, a model system that is well suited for this purpose. A core aim is todevelop a high resolution optical assay of vesicular release by applying new confocal methods to acute slices from transgenic mice expressing synaptopHluorin. This and recent advances in patching presynaptic terminals will be used to characterize, systematically, vesicle supply, Ca2+-dependenceof release and vesicle recycling. A kinetic model of the vesicle cycle will bedeveloped to elucidate the key determinants of synaptic function. The molecular determinants of specific presynaptic processes will be identified bycomparing model predictions with the behaviour of synapses when protein interactions are altered in transgenic mice or with peptides. Postsynaptically, AMPA receptor function will be examined with localized glutamate uncaging. Key subsynaptic processes will be linked to function by
Understanding the representation and storage of information in the mammalian brain requires knowledge of how single neurons contribute to generating patterns of network activity and how these patterns are modified by experience. In this proposal I will link cellular mechanisms of synaptic integration and plasticity to the functional behaviour of neuronal networks in the intact rodent cerebellar cortex. Experiments will focus on dendritic signalling in the three major inhibitory cell types in cerebellar cortex: Purkinje neurons, molecular layer interneurons, and Golgi cells. This will be addressed first in slice preparations using a combination of dendritic patch-clamp recordings and imaging of calcium and voltage-sensitive dye signals. These experiments will be linked to the network level by making targeted patch-clamp recordings from labelled neurons in vivo to study their input-output relationships during integration of different types of sensory input (auditory, visual and somatosensory). The spatiotemporal dynamics of activity in identified populations of neurons will be examined via optical imaging in conjunction with 2-photon imaging of calcium signals in single neurons and populations of neurons. Finally, I will use these tools to identify the locus of plasticity in the neural circuits of the cerebellum triggered by behaviourally relevant patterns of activity.
Cellular and molecular mechanisms of central chemosensory control of breathing. Central chemosensitivity and the reaction theory revisited. 05 Apr 2006
Breathing is the vital rhythmic activity which supports life of an individual by maintaining appropriate rates of oxygen uptake and CO2 elimination. This project addresses one of the most fundamental processes in respiratory physiology - central respiratory CO2 chemosensitivity, which is essential to adjust breathing to the needs of metabolism. Despite significant progress in this field the specific mechanisms of central respiratory chemosensitivity remain largely unknown. In order to pinpoint these mechanisms I propose to usea unique combination of experimental models ranging from cell culture to in vivo animal preparations. Cutting-edge optical imaging and electrophysiological recording techniques will be used to re-evaluate the relative roles of CO2, H+, and HCO3- as potential stimuli for central respiratory chemoreceptors. I shall then identify within the brainstem the populations of cells which respond first to physiologically relevant chemosensory stimulation in physiologically appropriate experimental conditions. To determine how the chemosensory stimulus is transduced I shall use pharmacological approaches to screen through potential intracellular and membrane targets to identify the mechanisms responsible for cellular chemosensitivity. When the candidate central respiratory chemoreceptors and putative chemosensory transduction mechanisms are identified, their physiological roles in mediating respiratory responses to CO2 will be tested using in vivo models.
Regulation of lung fibroblast and epithelial cell apoptosis by cyclooxygenase-2 and prostaglandin E2 and their role in the pathogenesis of pulmonary fibrosis. 06 Dec 2005
Pulmonary fibrosis represents the end stage of a heterogeneous group of conditions with poor prognosis and no effective treatment. Recent studies suggest increased epithelial cell (EC) apoptosis and fibroblast resistance to apoptosis contributes to the pathogenesis of fibrosis but the mechanisms are incompletely understood. However, the host laboratory has shown that patients with idiopathic pulmonary fibrosis (IPF) have a decreased capacity to synthesise cyclooxygenase (COX)-2 and prostaglandin E2 (PGE2). COX-2/PGE2 induce fibroblast apoptosis and protect epithelial cells from apoptosis but their role in regulating apoptosis in fibrotic lung is unknown. I therefore hypothesise that the decreased capacity to induce COX-2/PGE2 in patients with IPF contributes to pathogenesis by increasing EC apoptosis and decreasing fibroblast apoptosis. To address this hypothesis I will determine whether COX-2/PGE2 deficiency contributes to human fibrotic lung fibroblast resistanceto apoptosis and induction of EC apoptosis in vitro. I will also examine the effect of COX-2 deficiency on EC and fibroblast apoptosis in an animal model
Understanding the significance of the AIPL1:NUB1 interaction for photoreceptor homeostasis 20 Oct 2005
Mutations in the pineal- and photoreceptor-specific aryl hydrocarbon receptor interacting protein-like 1 (AIPL1) gene cause a devastating disease characterized by congenital blindness called Leber congenital amaurosis (LCA). The molecular basis of disease in LCA caused by AIPL1 mutations is not understood. It has been suggested that AIPL1 may function as a chaperone for phosphodiesterase (PDE) and farnesylated proteins. However, mutations in PDE subunits themselves lead to retinitis pigmentosa (RP) and global defects in the processing of farnesylated proteins were not observed in AIPL1 animal models. We have shown that AIPL1 can modulate the nuclear translocation and inclusion formation of the NEDD8 ultimate buster protein 1 (NUB1) and that this activity is affected by certain pathogenic mutations. NUB1 associates with the proteasome and targets small ubiquitin-like protein (NEDD8 and FAT10) conjugated proteins for degradation, providing a functional link between AIPL1 and the proteasome. However, the role of NUB1 in the retina is unknown. The primary goals of this study are therefore i) to determine the molecular mechanisms involved in the AIPL1-mediated regulation of NUB1 nuclear translocation ii) to determine the effect of AIPL1 on NUB1-mediated proteasomal degradation and downstream targets of NUB1 and iii) to determine whether these mechanisms are involved in the processing of PDE and farnesylated proteins by AIPL1, potentially establishing a relational link between the various pathways thus far implicated in AIPL1 LCA. Through these investigations we will gain a better understanding of the molecular mechanisms of AIPL1 LCA, which may identify novel targets for therapeutic intervention.
Signals from adipose tissue may underlie the relationship between obesity and metabolic diseases through their effects on insulin sensitivity and endothelial function. Asymmetric dimethylarginine (ADMA) is a novel risk factor for cardiovascular disease that inhibits nitric oxide bioavailability and causes endothelial dysfunction. ADMA is primarily cleared by catabolism through the activity of dimethylarginine dimethylaminohydrolase (DDAH). We found that adipose tissue expresses DDAH to high levels and generates significant amounts of ADMA, and the release is modifiable by changes in weight and insulin sensitizers. We propose to investigate the ADMA/DDAH pathway in adipose tissue of DDAH-1 +/- mice, and their wild-type littermates,to explore its relationship to the development of endothelial dysfunction in diet-induced obesity and to assess the reversibility of these changes by weight loss. Adipose tissue distribution and detailed quantification of changes in energy expenditure will be determined, as well as organ cultures toevaluate adipose ADMA secretion. Understanding the effects of the dynamic changes in weight on the adipose tissue DDAH/ADMA pathway and its regulation will increase our understanding of this novel product of this organ, explain the close link between body fat and endothelial dysfunction and provide a valuable basis for designing strategies in the treatment of obesity-associatedpathologies.
We have recently found that NMDA receptor-dependent long-term potentiation (LTP) occurs in about half of GABAergic feed-forward inhibitory interneurons in stratum radiatum of the hippocampus. This is only detected if interneurons are recorded in perforated-patch mode, and is not seen if whole-cell pipettes are used, possibly explaining why the phenomenon has not previously been reported. LTP in aspiny interneurons has extensive repercussions for the interaction between memory encoding and information processing in the corticalmicrocircuitry. However, the focus of this application is the underlying cellular mechanisms. Are postsynaptic action potentials required for LTP induction? Can LTP-competent interneurons be identified electrophysiologicallyor anatomically? Can interneurons switch from LTP-incompetence to LTP-competence? What is the role of tyrosine phosphorylation of NMDA receptors? What is the induction cascade downstream of NMDA receptors? How do sub-cellular Ca2+ microdomains relate to pathway-specific LTP in aspiny cells?Do interneurons exhibit NMDA receptor-dependent long-term depression (LTD)? What are the roles of NR2A- and NR2B-containing NMDA receptors, Ca2+/calmodulin kinases, and calcineurin in LTP (and LTD) in interneurons?
An estimated 800 bacterial species live in the oral cavity of Homo sapiens. The interaction between the commensal microbiota and its human host results in the commonest bacterial diseases of man; dental caries and periodontal diseases. A major bar to studying the orgal microbiota, whichis probably the easiest such microbial community to analyse, is the fact that 50% or more of the bacteria are uncultivable. One method of analysis which overcomes the need for culture and can enable the whole assemblage of oral microorganisms to be studied is metagenomics. We plan to construct a representative metagenomic library of the human oral microbiota and in this preliminary study analyse it for two groups of genes important for the maintenance of oral biofilms and the evolution of virulence and antibiotic resistance. Specifically, this library will be screened to identify genes encoding adhesins important in biofilm formation and for genes encoding systems involved in horizontal gene transfer. Results obtained will help in developing novel anti-plaque strategies and for understanding the ability of oral bacteria to act as reservoirs for antibiotic resistance genes and to spread these resistance genes among themselves and beyond the oral environment.
We have shown that EGF stimulation promotes multivesicular endosome/body (MVB) formation and inward vesiculation within MVB. MVB formation requires the ESCRT1 component, TSG101, whilst EGF stimulated inward vesiculation within MVB is totally dependent on tyrosine phosphorylation of annexin 1. EGF stimulation promotes the association of annexin 1 with MVB and annexin 1 accumulates with the EGFR on the internal vesicles of MVB. We propose to determine what regulates the enhanced association of annexin 1 with MVBs in EGF-stimulated cells, focusing upon the roles of the N-terminal domain of annexin 1, association of annexin 1 with the EGF receptor and interactions of annexin 1 with inositol phospholipids. We will then determine the molecular mechanisms underlying annnexin 1-mediated inward vesiculation. We will determine the role of the N-terminus of annexin 1 and whether the annexin 1 ligand, S100-A11, or proteolysis of annexin 1 are required. By performing qualitative and quantitative electron microscopy on annexin 1 knockout cells in which annexin 1 mutants have been expressed, and on wild type cells in which dominant negative annexin 1 mutants have been expressed, we will determine at which step(s) in the inward vesiculation process annexin 1 operates.
Cellular senescence is an irreversible program of cell cycle arrest that is triggered in normal somatic cells in response to a variety of intrinsic and extrinsic stimuli including alteration in telomere length and structure, DNA damage, physiological stress and activation of certain oncogenes. It can compromise tissue repair and regeneration and contribute to tissue and organismal ageing due to depletion of stem/progenitor cell compartments. It can also lead to removal of defective and potentially cancerous cells from the proliferating pool thereby preventing tumour development. The underlying mechanism that controls cellular senescence and the signal transduction pathways involved are not fully understood. We have developed a novel human mammary fibroblast cell system for dissecting the telomere-independent pathways that underlie this process and initiated a systematic analysis to identify the associated changes in the transcriptome. Our aim is to functionally validate genes that we have already identified, extend the transcriptional profiling to encompass all human genes and to carry out a genome wide gain of function RNA interference screen. Collectively, implementation of these strategies will enable us to dissect the telomere independent activities and pathways critical for regulating the finite proliferative potential of normal human cells.
Neuronal thalamic gap junctions: identity, location and role in slow EEG rhythms of (patho)physiological states 20 Oct 2005
Synchronized activity among thalamic and cortical neurones underlies the EEG expression of different behavioural state-dependent rhythms, whereas its alterations may lead to EEG paroxysms such as the spike-and-wave discharges (SWDs) of absence epilepsy. Our in vitro studies have identified a key role for gap junctions (GJs) among the glutamatergic thalamocortical (TC) neurones in the expression of synchronized, low-frequency thalamic oscillations, that define two behavioural states, i.e. the alpha rhythm and the slow (<1 Hz) sleep rhythm. In addition, connexin 36 (Cx-36)-based GJs among GABAergic nucleus reticularis thalami (NRT) neurones is known to support synchronized oscillations in this thalamic nucleus in vitro. Here we propose:1. to identify in vivo the contribution of GJs among TC neurones and among NRT cells to the expression of SWDs and of three EEG rhythms: the alpha rhythm, sleep spindles and the slow (<1 Hz) sleep rhythm;2. to identify the sites of GJ coupling in TC and NRT neurones, and the molecular identity of the Cx(s) present in TC neurones using electron microscopy, and triple labelling of dye-coupled neurones and immunocytochemistry with specific Cx antibodies.This multi-disciplinary approach from two laboratories with established expertise in their respective field will shed light into the role of thalamic GJs in EEG rhythms of fundamental importance in health and in one of the generalized epilepsies.